> I developed multiple sclerosis in 1991 and, over a two year period,
> gradually overcame it using an alternative treatment suggested by Edgar
Way back, on ththe MS newsgroup, a woman ordered information that said he'd
hadn't been diagnosed.
(see below). He's also posting mostly the same stuff to a bunch of other
illness related newsgroups.
Guard your pocketbooks, don't believe everything you read on the internet.
J
Apr 16 1998, 2:00 am
Newsgroups: alt.support.mult-sclerosis
From: Marilyn Bachmann <Marilyn.Bachm...@InternetMCI.com>
Date: 1998/04/16
Subject: CAYCE
My info on MS and Cayce's readings came from two sources -
A.R.E (Association for Research and Enlightment)
P.O. Box 595
Virginia Beach Virginia 23451
These are the people that keep the entire Cayce files (which is on CD rom
these days). I asked if they could send me anything that Cayce said about
MS - I think I included a donation of $10.00 or something like that to
cover costs and they sent me a packet of distilled information on what he
had to say.
Also,a Dr. Dudley Delany wrote a book called The Edgar Cayce Way of
Overcoming Multiple Sclerosis: Vibratory Medicine published by G&R
Publishing 1-800-383-1679 and he has a lot of info in this book, though to
be truthful I found the packet from A.R.E. more interesting. Delany was
never diagnosed and says he overcame MS using Cayce's methods, but that
lack of diagnosis nags at me.
candi bowen - 23 Jan 2006 22:59 GMT
Coincidentally, I visited the Edgar Cayce website last week for lupus info &
I was really put off by the fact that you had to pay (a lot) to join. Or to
get any info. I've read many of his books & I think he was really legit but
what's happened after he died? Understandably, they need funding to keep the
Cayce Foundation in VA Beach going, but I'm interested in how much money
they have coming in vs. going out & they should maybe explain that on their
home page. I don't think Edgar Cayce would ever withhold his readings if
someone couldn't afford it.
Candi
> From: J <spamtrap@invalid>
> Newsgroups: alt.support.lupus
[quoted text clipped - 35 lines]
> never diagnosed and says he overcame MS using Cayce's methods, but that
> lack of diagnosis nags at me.
Jenn L - 25 Jan 2006 14:31 GMT
somthing I will dig for at the library
William R Thompson - 25 Jan 2006 15:17 GMT
> Coincidentally, I visited the Edgar Cayce website last week for lupus info
> &
[quoted text clipped - 3 lines]
> but
> what's happened after he died?
Well, he stayed dead, and the world didn't end in 1938, or 1998,
or at any other time that he prophesied--or maybe it did and
nobody told me.
Go to
http://www.edgarcayce.org/health/database/chdata/
click on "Diseases" and scroll down to the illness of
your choice. Cayce recommended four specific treatments
for lupus, which "may be helpful" and "can provide relief."
And of course, "The above information is not intended
for self-diagnosis or self treatment. Please consult a
qualified health care professional in applying the
information contained in the Cayce Health Database."
In other words, there's a very good reason why Cayce has
remained an obscure crackpot instead of becoming an
influential source or health care information: his advice
doesn't work.
--Bill Thompson
J - 26 Jan 2006 11:19 GMT
William R Thompson wrote:
> Well, he stayed dead, and the world didn't end in 1938, or 1998,
> or at any other time that he prophesied
Good point.
I think I saw grapes for stomach pain (on his webpage)- I suppose might help
for constipation.
Deadly advice for stomach cancer.
J